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1.
分析水稻品种‘沈农265’和‘丽江新团黑谷’杂交的F2群体基部第二节间茎秆机械强度与该节间形态和茎秆解剖结构的相关性,并对基部第二节间机械强度和相关性状进行QTL定位的结果表明:机械强度与茎粗、茎壁面积、茎壁厚度、大小维管束数目、大小维管束面积、大小维管束韧皮部面积、大小维管束木质部面积呈显著或极显著的正相关,与节间长度呈极显著的负相关,而与茎秆扁平率的相关不显著。采用复合区间作图,从研究的14个目标性状中检测到18个QTL。控制基部第二节间的抗折力的QTL检测到4个,位于第4、7、9和10号染色体上,可解释遗传变异的12%~23%。在第4和第7染色体上的相同区间上还同时检测到了控制茎壁性状和维管束性状QTL,贡献率在12%~21%之间。说明这两个位点是控制基部第二节间机械强度的重要区域,也是茎壁性状、维管束性状与机械强度高度正相关的遗传学基础。  相似文献   

2.
水稻茎秆形态结构特征和化学成分与抗倒伏关系综述   总被引:16,自引:0,他引:16  
水稻茎秆形态结构特征和化学成分与其抗倒伏性能相关。本文对水稻茎秆高度、茎秆基部第1、2节间长度、茎秆粗细、茎壁厚度、厚壁组织(机械组织)数量和强度、维管束数量、细胞壁纤维素和木质素含量、细胞中碳水化合物积累的数量、硅与钾的含量以及茎秆抗倒伏相关的QTL等与水稻的抗倒伏性的相互关系进行了综述,为水稻抗倒伏优良品种性状的选育提供参考。  相似文献   

3.
稻米粒形的QTL定位及上位性和QE互作分析   总被引:1,自引:0,他引:1  
利用'广陆矮4号'×'佳辐占'水稻重组自交系构建了SSR标记的遗传图谱.联合2007年和2008年获得的两组稻米粒长(GL)、粒宽(GW)、长宽比(L/W)数据应用混合线性模型方法进行QTL定位,并作加性效应、加性×加性上位互作效应以及加性QTL、上位性QTL与环境的互作效应分析.结果显示;(1)在加性效应分析中两个群体共检测到4个控制粒长的QTL,4个控制粒宽的QTL,5个控制长宽比的QTL,贡献率分别为13.81%、15.36%和 16.29%.(2)在上位互作效应分析中两个群体共检测到2对控制粒长的互作QTL,1对控制粒宽的互作QTL,3对控制长宽比的互作QTL,贡献率分别为5.77%、2.59%和7.42%.(3)环境互作检测中,发现共有13个加性QTL和4对QTL的加性×加性上位性与环境产生了互作效应.结果表明,上位性效应和加性效应都影响稻米粒形遗传,QE互作效应也对粒形有着显著的影响.  相似文献   

4.
籽粒充实度较差是当前水稻亚种间杂种优势利用中所面临的最大障碍之一。研究采用籼粳交(圭630×02428)来源的DH群体对水稻籽粒充实度进行QTL分析,检测到1个主效应QTL(qGP-7),该QTL位于第7染色体RZ978~RG404a~RG404c区间的大约26cM的染色体区段上,对籽粒充实度的贡献率为10%~15%。发现了2对"加性×加性"效应的互作QTL,对籽粒充实度的贡献率皆为20%左右,表明QTL的上位性是控制籽粒充实度的重要遗传基础之一。还对亚种间杂交稻育种中"以饱攻饱"的亲本选配策略作了讨论。  相似文献   

5.
以晋豆23栽培大豆(Glycine max)为母本、灰布支黑豆(ZDD2315,半野生大豆)为父本衍生出447个RIL群体,通过构建SSR遗传图谱及利用混合线性模型分析方法,对2年大豆小区产量及主要植物学性状进行QTL定位,并作加性效应、加性×加性上位互作效应及环境互作效应分析。结果显示,共检测到12个与小区产量、单株粒重、单株茎重、单株粒茎比、有效分枝、主茎节数、株高和结荚高度相关的QTL,分别位于A1、A2、H_1、I、J_2和M连锁群上。其中小区产量、株高、单株粒重、有效分枝和主茎节数均表现为遗传正效应,即增加其性状的等位基因来源于母本晋豆23。同时,检测到11对影响小区产量、单株粒重、单株茎重、株高和结荚高度的加性×加性上位互作效应及环境互作效应的QTL,发现22个QTL与环境存在互作。实验结果表明,上位效应和QE互作效应对大豆小区产量及主要农艺性状的遗传影响很大。进行大豆分子标记辅助育种时,既要考虑效应起主要作用的QTL,又要注重上位性QTL,这样有利于性状的稳定表达和遗传。  相似文献   

6.
茎秆是玉米植株重要的组成部分,与植株倒伏、籽粒产量密切相关。研究我国玉米茎秆性状变化趋势,探讨不同年代茎秆性状演变规律,为我国玉米抗倒伏及高产品种选育提供参考。本研究以20世纪60-90年代65个代表性玉米自交系为材料,调查植株茎高、穗位高、茎节数、穗位节、茎粗、茎秆含水量、茎秆含糖量7个茎秆性状,及其衍生的穗位系数(穗位高/茎高)和穗节系数(穗位节/茎节数),基于最佳线性无偏估计值,开展性状相关性分析及不同年代自交系茎秆性状演变规律研究。结果显示,玉米自交系间茎秆性状差异显著;不同年代的茎秆性状时代特征不明显;随着年代的更替,玉米茎高、穗位高、茎节数、穗位节呈下降趋势;20世纪60-90年代穗位高改良效果显著;80年代左右玉米茎秆粗细育种目标由粗壮型调整为纤细型,可能与合理密植、提高单产的育种目标有关;90年代,玉米茎秆含水量降低3个百分点,下降显著。总之,抗倒伏研究一直是我国玉米育种的重要研究方向,且穗位高改良效果显著,玉米茎节数、穗位节将成为玉米抗倒伏及高产研究中新的重要关注点,研究结果对玉米抗倒伏及高产育种具有重要的指导意义。  相似文献   

7.
利用双单倍体群体剖析水稻产量及其相关性状的遗传基础   总被引:23,自引:0,他引:23  
主效QTL、上位性效应和它们与环境的互作(QE)都是数量性状的重要遗传因素。利用籼粳交珍汕97/武育粳2号F1植株上的花药进行组织培养得到的190个双单倍体群体和179个微卫星标记,通过两年两重复田间试验,采用混合线性模型方法分析了9个控制水稻产量及其相关性状的遗传效应,得到57个主效QTL,41对上位性互作,8对QTL与环境的互作和7对上位性效应与环境的互作。单个主效QTL解释这些性状1.3%~25.8%的表型方差。各性状QTL的累积表型贡献率达11.5%~66.8%。大多数性状之间具有显著的表型相关性,相关性较高的性状之间常具有较多共同或紧密连锁的QTL。结果表明,基因的多效性或紧密连锁可能是性状相关的重要遗传基础。  相似文献   

8.
水稻生物学产量及其构成性状的QTL定位   总被引:4,自引:4,他引:0  
刘桂富  杨剑  朱军 《遗传学报》2006,33(7):607-616
QTL的加性效应、加性×加性上位性效应及它们与环境的互作效应是数量性状的重要遗传分量.利用IR64/Azucena的125个DH品系为群体,分析了水稻生物学产量及其两个构成性状干草产量和谷粒产量的遗传组成.用基于混合模型的复合区间作图(MCIM)方法进行QTL定位.检测到12个位点有加性主效应,27个位点涉及双位点互作,18个位点存在环境互作.结果表明水稻生物学产量和它的两个构成性状普遍存在上位性效应和QE互作效应.此外,还探讨了性状间相关的遗传基础.发现4个QTLs和一对上位性QTLs可能与生物学产量与干草产量之间的正相关有关.3个QTL可能与干草产量与谷粒产量之间的负相关有关.这些结果可能部分地解释了这3个性状相关的遗传原因.通过对水稻生物学产量及其两个构成性状所定位QTL的分析,加深了对数量性状QTL的认识.首先,QTL的上位性效应和QE互作效应是普遍存在的;其次,QTL的多效性或紧密连锁可能是遗传相关的原因,当QTL对两个性状作用的方向相同时可导致正向遗传相关,反之则为负向遗传相关,当有些QTL表现为同向作用而另一些QTL表现为反向作用时,则可削弱性状间的遗传相关性;第三,复合性状的QTL效应可分解为其组成性状的QTL效应,如果QTL对各组成性状的效应方向相反而相互抵消,可使复合性状的QTL效应不易被检测;第四,加性效应的QTL常参预构成上位性效应,而具有上位性效应的QTL并非都有加性主效应,表明忽略上位性的QTL定位方法会降低检测QTL的功效;最后,鉴别不同类型的QTL效应有利于指导育种实践,选择主效QTL适用于多环境,QE互作QTL适用于特定环境,对上位性QTL应强调选择基因组合而并非单个基因.  相似文献   

9.
水稻叶片性状和根系活力的QTL定位   总被引:12,自引:2,他引:10  
应用由247个株系组成的珍汕97B/密阳46重组自交系(RIL)群体及其分子标记连锁图谱,检测控制剑叶、倒二叶、倒三叶的5个形态性状和控制根系伤流量性状的数量性状座位(QTL)。在9个标记区间检测到控制叶片形态性状的24个QTL,LOD值为2.9~11.8,单个QTL的表型变异贡献率为4.0%~32.5%;分别检测到56对和4对控制叶片形态和根系活力的上位性互作,绝大多数互作发生在2个不表现加性效应的座位之间。与该群体产量性状QTL的研究结果相比较,发现控制叶片性状和根系活力的QTL与产量性状QTL往往处于相似的染色体区间。  相似文献   

10.
不同发育阶段大豆株高和茎粗QTL的动态分析   总被引:2,自引:0,他引:2  
利用中豆29×中豆32的重组自交系,以复合区间作图法对不同发育阶段的大豆株高和茎粗同时进行非条件和条件QTL定位,在11个连锁群检测到18个株高QTL,在9个连锁群检测到19个茎粗QTL。不同发育时期影响大豆株高和茎粗QTL的数量、加性效应和贡献率均不相同,QTL表达具有时序性和选择性,有些QTL仅表达1次,有些可多次连续表达。有3个株高QTL和1个茎粗QTL在3个年度重复表达,有6个株高QTL和2个茎粗QTL在2个年度重复表达。F连锁群上株高和茎粗QTL存在共位性,R1~R4期均有株高和茎粗QTL同时表达,但株高和茎粗QTL的增效基因不同,株高QTL表达次数多而茎粗QTL表达次数较少,前期(V4~R3)QTL表达数量多而后期(R4~R5)表达数量较少。株高和茎粗QTL的动态变化与表型相关分析结果一致,对于适期选择粗秆抗倒的高产材料具有指导作用。  相似文献   

11.
以旱稻品种IRAT109与水稻品种越富杂交构建的DH群体的116个株系及其亲本为材料,在水、旱2种栽培条件下种植,研究了稻米蒸煮和营养品质性状的变化规律,在水、旱2个土壤水分环境下对直链淀粉含量(AC)、胶稠度(GC)、碱消值(GT)和蛋白质含量(PC)4个蒸煮和营养品质性状进行QTL定位及QTLs与环境互作分析。结果表明,以上4个品质性状在水、旱2种不同栽培条件下差异较大,说明这些性状受水分条件影响较大,旱栽条件下稻米蒸煮和营养各品质性状均有不同程度的升高,其中蛋白质含量平均提高37.9%。QTL分析结果表明,4个稻米品质性状在2个环境中的表现型值都为连续分布,均存在超亲遗传类型,共检测到7个加性效应QTL与稻米蒸煮和营养品质性状4项指标有关,分别位于第1、2、3、6、8、11染色体上,单个QTLs对性状的贡献率在1.91%~19.77%之间。位于第3染色体上控制碱消值的QGt3,第6染色体上控制直链淀粉含量的QAc6,在2个不同土壤水分条件下均与环境存在显著互作,对环境互作的贡献率分别为8.99%和47.86%。控制直链淀粉含量的2对上位性QTLs与土壤水分环境显著互作,贡献率较大,分别为32.54%和11.82%。并筛选到5个主效QTL(QGt6b、QGt8、QGt11、QGc1和QPc2)在抗旱育种中可用于蒸煮和营养各品质性状MAS改良。  相似文献   

12.
To genetically dissect drought resistance associated with japonica upland rice, we evaluated a doubled haploid (DH) population from a cross between two japonica cultivars for seven root traits under three different growing conditions (upland, lowland and upland in PVC pipe). The traits included basal root thickness (BRT), total root number (RN), maximum root length (MRL), root fresh weight (RFW), root dry weight (RDW), ratio of root fresh weight to shoot fresh weight (RFW/SFW) and ratio of root dry weight to shoot dry weight (RDW/SDW). The BRT was significantly correlated with the index of drought resistance, which was defined as the ratio of yield under the stress of the upland condition to that under the normal lowland condition. A complete genetic linkage map with 165 molecular markers covering 1,535 cM was constructed. Seven additive quantitative trait loci (QTLs) and 15 pairs of epistatic loci for BRT and RN were identified under upland and lowland conditions, and 12 additive QTLs and 17 pairs of epistatic QTLs for BRT, RN, MRL, RFW, RFW/SFW and RDW/SDW were identified under the PVC pipe condition. Four additive QTLs and one pair of epistatic QTLs controlling IDR were also found. These QTLs individually explained up to 25.6% of the phenotypic variance. QTL × environment (Q × E) interactions were detected for all root traits, and the contributions of these interactions ranged from 1.1% to 19.9%. Five co-localized QTLs controlling RFW and RDW, RFW/SFW, RDW/SDW and IDR, BRT and RN, RN, MRL and IDR were found. Four types of QTLs governing BRT and RN were classified by their detection in the upland and lowland conditions. Some common QTLs for root traits across different backgrounds were also revealed. These co-localized QTLs and common QTLs will facilitate marker-assisted selection for root traits in rice breeding programs.  相似文献   

13.
不同供水条件下水稻幼苗根系形成的遗传分析   总被引:1,自引:0,他引:1  
利用分子标记图谱对溶液培养与旱作培养(纸培养)下的水稻(Oryza sativa L.)幼苗的种子根与最长不定根长,不定根数,总根干重,根冠比等性状进行了基因定位与遗传分析。4种参数共检测到6个数量性状位点(quantitative trait loci,QTLs)与22对上位性互作位点,其中溶液培养中的最长不定根长,总根干重和旱作培养中的总根干重检测到的QTLs位点对总变异的贡献率分别为20%,23%和13%左右;旱作培养中的最长不定根长,不定根数,根冠比和溶液培养中的根冠比仅检测到上位性位点,对表型变异的贡献率在12%-61%之间,溶液培养与旱作条件下没有一个或一对检测到的QTL或互作位点完全相同,提示溶液培养和旱作条件下影响幼苗根系生长的遗传机制差异,上位性作用对旱作培养条件下的根生长具重要影响。  相似文献   

14.
Addicive effects, additive by additive epistatic effects, and their environmental interactions of QTLs are important genetic components of quantitative traits. Genetic architecture underlying rice biomass yield and its two component traits (straw yield and grain yield) were analyzed for a population of 125 DH lines from an inter-subspecific cross of IR64/Azucena. The mixed-model based composite interval mapping approach (MCIM) was used to detect QTLs, There were 12 QTLs detected with additive main effects, 27 QTLs involved in digenic interaction with aa and/or aae effects, and 18 QTLs affected by environments with ae and/or aae effects. It was revealed that epistatic effects and QE interaction effects existed on biomass yield and its component traits in rice. In addition, the genetic basis of relationships among these traits were investigated. Four QTLs and one pair of epistatic QTLs were detected to be responsible for the positive correlation between biomass yield and straw yield. Three QTLs might be responsible for the negative correlation between straw yield and grain yield. This result could partially explain the genetic basis of correlation among the three traits, and provide useful information for genetic improvement of these traits by marker-assisted selection.  相似文献   

15.
为了研究不同水分条件下组成型根系性状和适应性根系性状的遗传机制,利用由IR64/Azucena发展的双单倍体(DH)群体分析了淹水和干旱条件下水稻幼苗种子根长(SRL)、不定根数(ARN)、总根干重(RW)及其对应的相对参数(干旱和淹水条件下根系性状的比值)的QTLs。淹水与干旱条件下检测到一个共同的种子根长QTL和一个共同的总根干重QTL。同时对前人发表的遗传群体定位的根系性状QTLs进行比较分析,检测到几个共同的根系性状QTLs。对与细胞伸长、分裂相关的候选基因进行了定位,其中4个细胞壁相关的ESTs(OsEXP2,OsEXP4,EXT和Xet)被定位在与不同水分条件下检测出的根系性状QTLs的相同区间。  相似文献   

16.
To understand the genetic background of root growth of rice (Oryza sativa L.) seedlings under different water supply conditions, quantitative trait loci (QTLs) and epistatic effect on seminal root length, maximum adventitious root length, adventitious root number, total root dry weight and ratio of root to shoot were detected using molecular map including 103 restriction fragment length polymorphism (RFLP) markers and 104 amplified fragment length polymorphism (AFLP) markers mapped on a recombinant inbred line (RIL) population with 150 lines derived from a cross between an lowland rice IR1552 and an upland rice Azucena in both solution culture (lowland condition) and paper culture (upland condition). Six QTLs and twenty-two pairs of epistatic loci for the four parameters were detected. Three QTLs detected for maximum adventitious root length in solution culture (MARLS), total root dry weight in both solution culture and paper culture (TRDWS and TRDWP) accounted for about 20%, 23% and 13% of the total variations, respectively. Only epistatic loci were found for maximum adventitious root length and adventitious root number in paper culture (MARLP and ARNP), and for ratio of root to shoot in both paper and solution culture (R/SP and R/SS), which accounted for about 12%-61% of the total variations in the parameters, respectively. No identical QTL or epistatic loci were found for the parameters in both solution and paper culture. The results indicate that there is a different genetic system responsible to root growth of rice seedlings under lowland and upland conditions and epistasis might be the major genetic basis for MARLP, ARNP, R/SP and R/SS.  相似文献   

17.
To investigate the genetic factors underlying constitutive and adaptive root growth under different water-supply conditions, a double haploid (DH) population, derived from a cross between lowland rice variety IR64 and upland rice variety Azucena, with 284 molecular markers was used in cylindrical pot experiments. Several QTLs for seminal root length (SRL), adventitious root number (ARN) and total root dry weight (RW) respectively, under both flooding and upland conditions were detected. Two identical QTLs for SRL and RW were found under flooding and upland conditions. The relative parameters defined as the ratio of parameters under the two water-supply conditions were also used for QTL analysis. A comparative analysis among different genetic populations was performed for the QTLs for root traits and several consistent QTLs for root traits across genetic backgrounds were detected. Candidate genes for cell expansion and elongation were used for comparative mapping with the detected QTLs. Four cell wall-related expressed sequence tags (ESTs) for OsEXP2, OsEXP4, EXT and Xet were mapped on the intervals carrying the QTLs for root traits.  相似文献   

18.
Drought is the major abiotic stress limiting rice (Oryza sativa) production and yield stability in rainfed lowland and upland ecosystems. Root systems play an important role in drought resistance. Incorporation of root selection criteria in drought resistance improvement is difficult due to lack of reliable and efficient screening techniques. Using a wax-petrolatum layer system simulated to compacted soil layers, root traits were evaluated in a doubled haploid (DH) population derived from the cross between 'IR64' and 'Azucena'. Twelve putative QTLs (quantitative trait loci) were detected by interval mapping comprising four QTLs for root-penetration ability, four QTLs for root thickness, two QTLs for penetrated root number, and two QTLs for total root number. These QTLs individually explained 8.4% to 16.4% of the phenotypic variation. No QTL was detected for maximum penetrated root length by interval mapping. One QTL located between RG104 and RG348 was found to influence both root-penetration ability and root thickness. QTLs for root-penetration ability and root thickness were compared across two populations, 'IR64'-'Azucena' and 'CO39'-'Moroberekan', and different testing conditions. The identified consistent QTLs could be used for marker-assisted selection for deep and thick roots with high root-penetration ability in rice.  相似文献   

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